| Tag | Content |
|---|
EnhancerAtlas ID | HS047-30243 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr7:1208980-1210040 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr7:1209683-1209702 | CAGCTCCCCCTGGCGGCAG | - | 6.09 | | INSM1 | MA0155.1 | chr7:1209642-1209654 | CGCCCCCTTGCA | - | 6.02 | | KLF14 | MA0740.1 | chr7:1209637-1209651 | GGCCACGCCCCCTT | + | 8.42 | | KLF16 | MA0741.1 | chr7:1209638-1209649 | GCCACGCCCCC | + | 6.62 | | SP1 | MA0079.4 | chr7:1209635-1209650 | CCGGCCACGCCCCCT | + | 6.19 | | SP3 | MA0746.2 | chr7:1209637-1209650 | GGCCACGCCCCCT | + | 6.82 | | SP4 | MA0685.1 | chr7:1209635-1209652 | CCGGCCACGCCCCCTTG | + | 6.59 | | SP8 | MA0747.1 | chr7:1209638-1209650 | GCCACGCCCCCT | + | 6.92 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_35540 | chr7:1208673-1210137 | HepG2 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I001169 | chr7 | 1208950 | 1210250 |
|
Enhancer Sequence | ATTCATCATC TTTAGGCATG CGAGCTTCTC CTACCTCTAT CCATCCTTCC TTCAGCCCAT 60
TTCCCCCGAC TTCTGCCACC ACCTCCGGGA CGTCCTGAAG GCGAACCGGC CTCCCACCTG 120
CTAAGTCCAA CAGACACTTC AGCCTGGCTC TCACCAGCCA TGGCGGGTTG CCCTCCTACC 180
TCTTGACAAC ACGCTCTTCC TCGGCTGCAG AGACACCTCC TCTCCGTATT TTCCTCCCAC 240
ATTAGCAATG ACCACACTCA GGCTATGTCA CTCATGGTAT TTTTGCATCA GAAATGCCAT 300
CCTTGGGCCG GGCGCCATGC CTCATGCCTG TAATCCCAGC GCTTTGAGAG GCCGAGCCGG 360
GTGGATCCCT TGAGGCCAGG AGTTCAAAAA CGGCCTGGGC AACATAGCAA GACCCTGTCT 420
CTACAAAAAG AAACAGTTTT TAAGTCATTC CTGATTTTAC AACGCTACTC TGATCTGAGC 480
CCCTGTGGCC TCGGGATCCC CAGGCGTCTG TTCCCGAGAA CGCGGGGCAG AAAGCCTAGT 540
CCTGCACGCA GTACCAACAA TGCGGAGTCA GCGGGTTGTT TCGACTTTGT TCTGTTTCCT 600
GAGGGGTTCT GAATAAGGGC CACCCCCTTC CTCCTCTGTG CCGCCATGTT CCCTCCCGGC 660
CACGCCCCCT TGCAACCCCT CCAATCTCCG CCCTGCACCC TGGCAGCTCC CCCTGGCGGC 720
AGCAGCGGGT CTTCGTGGAG TCAGCCCCTC CGCTGCTTGG CCGCTGGGTT TGTCCCTTAT 780
TTTAATGGAT GCGCGTTGGC TAGGACTGCA ACATTGTTTC TTTCTTCCAC AAATTTTAGT 840
TTGAAACAGA CAGGAAGTTA ATTTCCCGTC TGGCTGCCAC ACCTGCTGGT GGCGTGGACT 900
GCGGCCCTTA GGCTGTTCCT TGCTCGATTT AACCCTGGGA GACATCGAAG CCTTCCCACC 960
CAAGCTGTAG GGAGCTGTTG AAGACCTGGT TCACACGAGA TCCTTTGCGG GGTGCAGCTG 1020
GGGAAAGCAT GATTTCAGCT TGTAAGCTGC ATGGAGAATG 1060
|
